US5176842A - Method of manufacturing a resin bound magnet - Google Patents
Method of manufacturing a resin bound magnet Download PDFInfo
- Publication number
- US5176842A US5176842A US07/635,270 US63527090A US5176842A US 5176842 A US5176842 A US 5176842A US 63527090 A US63527090 A US 63527090A US 5176842 A US5176842 A US 5176842A
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- United States
- Prior art keywords
- magnet
- resin
- magnetic material
- resin bound
- epoxy resin
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- Expired - Lifetime
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- 229920005989 resin Polymers 0.000 title claims abstract description 48
- 239000011347 resin Substances 0.000 title claims abstract description 48
- 238000004519 manufacturing process Methods 0.000 title abstract description 7
- 239000003822 epoxy resin Substances 0.000 claims abstract description 32
- 229920000647 polyepoxide Polymers 0.000 claims abstract description 32
- 239000000696 magnetic material Substances 0.000 claims abstract description 29
- 229920001971 elastomer Polymers 0.000 claims abstract description 21
- 239000005060 rubber Substances 0.000 claims abstract description 21
- 229920000459 Nitrile rubber Polymers 0.000 claims abstract description 6
- 229920002857 polybutadiene Polymers 0.000 claims abstract description 6
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims abstract 4
- 150000001875 compounds Chemical class 0.000 claims description 24
- 229910052761 rare earth metal Inorganic materials 0.000 claims description 16
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 13
- -1 triazine compound Chemical class 0.000 claims description 9
- 229910052742 iron Inorganic materials 0.000 claims description 6
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 5
- 229910052796 boron Inorganic materials 0.000 claims description 5
- 229910017052 cobalt Inorganic materials 0.000 claims description 3
- 239000010941 cobalt Substances 0.000 claims description 3
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 3
- 238000005260 corrosion Methods 0.000 claims description 2
- 230000007797 corrosion Effects 0.000 claims description 2
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 claims 1
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims 1
- 150000001639 boron compounds Chemical class 0.000 claims 1
- 230000005494 condensation Effects 0.000 claims 1
- 238000009833 condensation Methods 0.000 claims 1
- 239000008240 homogeneous mixture Substances 0.000 claims 1
- 230000006835 compression Effects 0.000 abstract description 12
- 238000007906 compression Methods 0.000 abstract description 12
- 238000004898 kneading Methods 0.000 abstract description 10
- 239000000203 mixture Substances 0.000 abstract description 8
- 238000002156 mixing Methods 0.000 abstract description 6
- 238000000465 moulding Methods 0.000 abstract description 6
- 238000012644 addition polymerization Methods 0.000 abstract description 5
- 238000000034 method Methods 0.000 description 18
- 239000011230 binding agent Substances 0.000 description 17
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 14
- 239000003960 organic solvent Substances 0.000 description 8
- 239000002245 particle Substances 0.000 description 8
- 239000000463 material Substances 0.000 description 7
- 150000002910 rare earth metals Chemical class 0.000 description 7
- 239000002904 solvent Substances 0.000 description 6
- 238000011282 treatment Methods 0.000 description 6
- 238000000576 coating method Methods 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 239000005062 Polybutadiene Substances 0.000 description 4
- 150000003918 triazines Chemical class 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- 229910052779 Neodymium Inorganic materials 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000748 compression moulding Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000000314 lubricant Substances 0.000 description 3
- 239000006247 magnetic powder Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 229910052723 transition metal Inorganic materials 0.000 description 3
- 150000003624 transition metals Chemical class 0.000 description 3
- 238000001291 vacuum drying Methods 0.000 description 3
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 2
- 239000008116 calcium stearate Substances 0.000 description 2
- 235000013539 calcium stearate Nutrition 0.000 description 2
- 229910001873 dinitrogen Inorganic materials 0.000 description 2
- 238000004070 electrodeposition Methods 0.000 description 2
- 238000009998 heat setting Methods 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- 239000004570 mortar (masonry) Substances 0.000 description 2
- QEFYFXOXNSNQGX-UHFFFAOYSA-N neodymium atom Chemical compound [Nd] QEFYFXOXNSNQGX-UHFFFAOYSA-N 0.000 description 2
- 229910001172 neodymium magnet Inorganic materials 0.000 description 2
- 239000011368 organic material Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000004381 surface treatment Methods 0.000 description 2
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- 229910052777 Praseodymium Inorganic materials 0.000 description 1
- 101100386054 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) CYS3 gene Proteins 0.000 description 1
- 229910052772 Samarium Inorganic materials 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 150000004662 dithiols Chemical group 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical class C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- PUDIUYLPXJFUGB-UHFFFAOYSA-N praseodymium atom Chemical compound [Pr] PUDIUYLPXJFUGB-UHFFFAOYSA-N 0.000 description 1
- KZUNJOHGWZRPMI-UHFFFAOYSA-N samarium atom Chemical compound [Sm] KZUNJOHGWZRPMI-UHFFFAOYSA-N 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 101150035983 str1 gene Proteins 0.000 description 1
- 229910052727 yttrium Inorganic materials 0.000 description 1
- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
- H01F1/00—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
- H01F1/01—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials
- H01F1/03—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity
- H01F1/032—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of hard-magnetic materials
- H01F1/04—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of hard-magnetic materials metals or alloys
- H01F1/047—Alloys characterised by their composition
- H01F1/053—Alloys characterised by their composition containing rare earth metals
- H01F1/055—Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5
- H01F1/057—Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5 and IIIa elements, e.g. Nd2Fe14B
- H01F1/0571—Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5 and IIIa elements, e.g. Nd2Fe14B in the form of particles, e.g. rapid quenched powders or ribbon flakes
- H01F1/0575—Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5 and IIIa elements, e.g. Nd2Fe14B in the form of particles, e.g. rapid quenched powders or ribbon flakes pressed, sintered or bonded together
- H01F1/0578—Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5 and IIIa elements, e.g. Nd2Fe14B in the form of particles, e.g. rapid quenched powders or ribbon flakes pressed, sintered or bonded together bonded together
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/90—Magnetic feature
Definitions
- This invention relates to a method for manufacturing a resin bound magnet. More particularly, it relates to a method for manufacturing a resin bound magnet having excellent strength and magnetic characteristics, and magnets produced therefrom.
- a resin bound magnet is normally composed of a powdered magnetic material and a binder resin material for binding the fine particles of the magnetic material.
- the powdered magnetic material is typically a combination of rare earth and transition metals, such as, samarium and cobalt (Sm-Co), or of neodymium, iron and boron (Nd-Fe-B), while the binder resin material is normally a solid epoxy resin (see Japanese Patent Publications, Tokkai Hei No. 1-114006 and No. 2-6573).
- the resin bound magnet is typically prepared in the following manner.
- the solid epoxy resin is first heated and then dissolved in an organic solvent, such as, acetone containing a hardening agent.
- the powdered magnetic material is then added to this solution. Thereafter, the solution is mixed well and kneaded while dry nitrogen gas is blown into the solution to vaporize the solvent.
- the residue is then dried by using a vacuum dryer and the dried blocks of the compound are pulverized to powder form.
- the powder is passed through a sieve to produce particles with a substantially uniform granule size, which are then filled into a metal mold for compression molding.
- the molded body is then subjected to treatment to eliminate any powdery residue, heat-set the resin and other conventional supplementary treatments.
- the solid epoxy resin since the solid epoxy resin is relatively insoluble in organic solvents at ambient temperature, it must be heated to accelerate its dissolution.
- the amount of the powdered compound introduced into the compression metal mold can fluctuate depending on the solvent content of the compound. This results in inaccuracies in the amount of material introduced into the mold as well as the density and strength of the product.
- These problems hinder the preparation of a resin bound magnet having a relatively large diameter, reduced thickness, or length, wherein the powdered compound must be very evenly filled with the mold.
- the prior art resin bound magnets did not exhibit sufficient radial compression strength, they could not be press fit into a rotor. Consequently, the magnets needed to be fitted to the rotor by using an adhesive agent. This resulted in reduced efficiency and increased costs.
- the invention is achieved by mixing and kneading a powdered magnetic material with a rubber modified epoxy resin obtained from the addition polymerization of an epoxy resin and a butadiene rubber or a nitrile rubber and thereafter, molding and setting the kneaded mixture into the desired shape.
- the amount of the rubber component in the inventive modified epoxy resin should be from about 5.0 to 30 weight percent to provide a resin having the properties desired to produce the results of the present invention.
- Rubber modified epoxy resins prepared through addition polymerization of an epoxy resin and a butadiene rubber or a nitrile rubber exhibit a permanent deformation under a low pressure force, are soft and heat-resistive, yet are highly elastic, possess low dynamic exothermic properties and excellent low-temperature characteristics.
- the inventive resin bound magnets exhibit excellent radial compression strength and mechanical properties.
- neither rigorous control of the organic solvent nor a vacuum drying process are required. Consequently, the inventive compound of the magnetic material and the rubber modified epoxy resin is highly workable.
- FIG. 1 is a schematic flow chart of the method of the invention.
- FIG. 2 is a structural formula of the rubbery portion of a modified epoxy resin suitable for use as a binder in the present invention.
- the powdered magnetic material of the invention may contain a powdered compound of a rare earth metal, iron and boron, such as, Nd-Fe-B as its principle ingredient.
- a powdered compound of a rare earth metal and cobalt, such as, Sm-Co may be used.
- the rare earth component of the compound may be a mixture of rare earth elements selected from the group consisting of light rare earth elements and heavy rare earth elements, e.g., La through Lu (atomic numbers 57 through 71), Sc and yttrium (Y).
- the powdered compound contains at least one light rare earth element, such as, neodymium (Nd) or praseodymium (Pr) that is readily available at a relatively low cost.
- the content of rare earth elements in the compound is preferably between about 12 and 20 atom percent.
- the iron (Fe) content of the powdered magnetic material is preferably between about 65 and 82 atom percent, whereas the boron (B) content is advantageously between about 4 and 24 atom percent.
- the powdered magnetic material is typically a rare earth element-iron-boron compound which is expressed by the formula:
- the powdered magnetic material has a particle size distribution such that about 0.1 wt. percent or less has a size equal to or greater than about 420 ⁇ m, and no more than about 15 wt. % have a particle size equal to or less than about 44 ⁇ m. This facilitates mixing the compound with a binder resin material at a high concentration.
- the particles of the powdered magnetic material are preferably coated with a rust-preventive agent before mixing and kneading with the binder resin material, since the powdered magnetic material containing rare earth elements, iron and boron, is easily oxidized and has poor corrosion-resistance.
- a surface treatment can significantly improve the corrosion-resistance of the powder and make the process of rust-prevention after molding less troublesome.
- the coating process using a triazine derivative e.g., dibutylamino-triazine-dithiol, as disclosed in Japanese Patent Publication Tokkai Hei No. 1-114006 by the applicant of the present invention, may be advantageously used.
- each of the atoms of the heavy metals, i.e., Fe, Nd, of the magnetic material are adsorption-bonded with the dithiol group of the triazine derivative so that the particle is coated with an organic material which is highly rust-preventive.
- the effect of the bridge formation carried by the organic compound and the binder resin can contribute to improvement in the mechanical strength of the molded body.
- a binder resin which can be used in the present invention is the rubber modified epoxy resin wherein the rubbery portion has the structural formula as shown in FIG. 2 wherein m is from 1 to 3, n is 1 to 3, and x is from 1 to 8, prepared by addition polymerization of an epoxy resin and a butadiene rubber or a nitrile rubber.
- binder resin suitable for use in the present invention has the structural formula: ##STR1## wherein p is 1 to 3, x is 1 to 8, m is 1 to 3 and n is 1 to 3,
- a preferred process for carrying out the method of manufacturing the inventive magnet from a powdered magnetic material (or a powdered magnetic material that has been subjected to a corrosion resistent treatment) and a rubber modified epoxy resin as binder, will be described by referring to FIG. 1.
- Kneading as used herein includes conditioning, mixing and physically kneading the powdered magnetic material and a binder resin to prepare the material to be molded for a permanent magnet.
- the magnetic powder is coated with a rubber modified epoxy resin prepared by the addition polymerization of an epi-bis type epoxy resin and a butadiene rubber or a nitrile rubber having a rubber content between about 5 and 30 wt. %, and preferably, about 20 wt. %.
- a rubber modified epoxy resin prepared by the addition polymerization of an epi-bis type epoxy resin and a butadiene rubber or a nitrile rubber having a rubber content between about 5 and 30 wt. %, and preferably, about 20 wt. %.
- the amount of binder resin is from 2 to 4 wt. % based on the weight of the magnetic material.
- the modified epoxy resin is mixed with a hardening agent and the mixture is dissolved in an organic solvent, e.g., acetone or methyl ethyl ketone, in which it is soluble.
- an organic solvent e.g., acetone or methyl ethyl ketone, in which it is soluble.
- the magnetic powder is admixed and kneaded with the solution and the solvent is removed, thereby coating the particles with the binder resin.
- the binder resin is dissolved in acetone in a non-magnetic mortar and the powdered magnetic material is added to the solution.
- the mixture is kneaded with a spatula while dry nitrogen gas (N 2 ) is blown into the solvent to prevent oxidation of the powdered magnetic material and to accelerate evaporation of the solvent.
- N 2 dry nitrogen gas
- a screw, or a floating or soft-mixing apparatus may be used for kneading.
- the product obtained from the kneading step is then pulverized in a non-magnetic mortar and passed through a 60-mesh sieve to obtain a powdered compound with even sized particles.
- a lubricant may be admixed with the sieved powdered compound.
- Suitable lubricants mixture include calcium stearate, zinc stearate, molybdenum and the like.
- the amount of lubricant is generally from about 0.01 to 0.5 wt. %.
- the mixture is then introduced into a metal mold to form a compression molded compound as described below.
- the mixture of the sieved compound and calcium stearate is introduced into a compression mold and subjected to a pressure of about 9 ton/cm 2 to obtain a ring-shaped or tablet-shaped compression-molded and resin-bound body.
- the molded body is subjected to a heat treatment at 200° C. for approximately 20 minutes for heat setting and to obtain a resin bound magnet.
- the prepared resin bound magnet may then subjected to a rust-prevention process using known spraying and electrodeposition, or immersion techniques to produce a finished product.
- the rust-prevention process may be omitted if the powdered magnetic material has been subjected to a coating process using a triazine derivative as described earlier. However, it is advisable that the resin bound magnet be further subjected to a triazine treatment for the protection of particles whose coating might have been destroyed during the molding process.
- This second triazine treatment process uses a triazine derivative similar to or the same as that described above to coat the molded magnet.
- the operation of coating the molded magnet with an organic material may be conducted by means of immersion, electrodeposition, or spray techniques.
- the inventive resin bound magnet prepared by the above process contains a highly rigid hard segment in which the molecules are firmly bound together and a soft segment constituted by a highly elastic rubber content, it exhibits a permanent deformation under a low compressive force and is soft and heat-resistive. Yet, the inventive magnet is highly elastic, and possesses a low dynamic exothermic property and excellent low-temperature characteristics. Moreover, the inventive resin bound magnet exhibits excellent radial compression strength and other mechanical properties.
- the kneaded compound can be easily reduced to powder because the rubber modified epoxy resin is essentially unaffected by the acetone in the compound.
- the compound does not need to be vacuum dried to remove the acetone.
- the Table below shows some of the binding characteristics of an epi-bis type epoxy resin containing a rubber modified epoxy resin in varying amounts as well as those of a conventional currently available epoxy resin.
- a resin bound magnet prepared by the method of the invention when used for a rotor magnet of an electric motor, it can be easily press fit into the motor. Motors provided with such a resin bound magnet are very light, exhibit excellent magnetic characteristics, and yet, can be produced at reduced manufacturing cost.
- the rubber modified epoxy resin is minimally or not affected by the residual organic solvent, such as, acetone, it does not need to be subjected to rigorous control of the residual organic solvent nor a vacuum drying process, and exhibits improved workability after compression molding.
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- Polymers & Plastics (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Power Engineering (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Inorganic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Hard Magnetic Materials (AREA)
- Manufacturing Cores, Coils, And Magnets (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Casting Or Compression Moulding Of Plastics Or The Like (AREA)
- Graft Or Block Polymers (AREA)
- Epoxy Resins (AREA)
- Powder Metallurgy (AREA)
Abstract
A method of manufacturing a resin bound magnet comprising, mixing and kneading a powdered magnetic material and a rubber modified epoxy resin obtained from the addition polymerization of an epoxy resin and a butadiene or nitrile rubber and thereafter molding and setting the kneading mixture into a desired shape. The magnets prepared by the present invention exhibit permanent deformation under low compressive force, are soft and heat resistant and yet highly elastic and possess low dynamic exothermic properties and excellent low temperature characteristics. In addition, the inventive magnets exhibit excellent radial compression strength and other mechanical properties.
Description
1. Field of the Invention
This invention relates to a method for manufacturing a resin bound magnet. More particularly, it relates to a method for manufacturing a resin bound magnet having excellent strength and magnetic characteristics, and magnets produced therefrom.
2. Description of the Prior Art
In recent years, in response to an increasing demand for powerful and miniaturized magnets to be used for electric motors, a variety of resin bound magnets obtained using rare earth and transition metals having excellent magnetic characteristics have been proposed.
A resin bound magnet is normally composed of a powdered magnetic material and a binder resin material for binding the fine particles of the magnetic material. The powdered magnetic material is typically a combination of rare earth and transition metals, such as, samarium and cobalt (Sm-Co), or of neodymium, iron and boron (Nd-Fe-B), while the binder resin material is normally a solid epoxy resin (see Japanese Patent Publications, Tokkai Hei No. 1-114006 and No. 2-6573).
When a solid epoxy resin is used as binder, the resin bound magnet is typically prepared in the following manner. The solid epoxy resin is first heated and then dissolved in an organic solvent, such as, acetone containing a hardening agent. The powdered magnetic material is then added to this solution. Thereafter, the solution is mixed well and kneaded while dry nitrogen gas is blown into the solution to vaporize the solvent. The residue is then dried by using a vacuum dryer and the dried blocks of the compound are pulverized to powder form. The powder is passed through a sieve to produce particles with a substantially uniform granule size, which are then filled into a metal mold for compression molding. The molded body is then subjected to treatment to eliminate any powdery residue, heat-set the resin and other conventional supplementary treatments.
While a rare earth/transition metal type resin bound magnet prepared according to the above known method exhibits excellent magnetic characteristics, allows a number of poles to be formed, is easily worked by machine tools and can have a desired configuration, it is accompanied by the following problems due to the solid epoxy resin binder.
Firstly, since the solid epoxy resin is relatively insoluble in organic solvents at ambient temperature, it must be heated to accelerate its dissolution.
Secondly, because residual organic solvent in the resultant compound produces significant adverse effects on the radial compression strength of the compound after molding, the amount of the organic solvent in the compound must be rigorously minimized by allowing the powdered compound to remain under vacuum for 24 hours after a vacuum drying of 2 hours.
In addition, the amount of the powdered compound introduced into the compression metal mold can fluctuate depending on the solvent content of the compound. This results in inaccuracies in the amount of material introduced into the mold as well as the density and strength of the product. These problems, in turn, hinder the preparation of a resin bound magnet having a relatively large diameter, reduced thickness, or length, wherein the powdered compound must be very evenly filled with the mold. Moreover, since the prior art resin bound magnets did not exhibit sufficient radial compression strength, they could not be press fit into a rotor. Consequently, the magnets needed to be fitted to the rotor by using an adhesive agent. This resulted in reduced efficiency and increased costs.
We have discovered a method for manufacturing a resin bound magnet which possesses improved radial compression strength and mechanical properties as compared with the prior art resin bound magnets. The invention is achieved by mixing and kneading a powdered magnetic material with a rubber modified epoxy resin obtained from the addition polymerization of an epoxy resin and a butadiene rubber or a nitrile rubber and thereafter, molding and setting the kneaded mixture into the desired shape. The amount of the rubber component in the inventive modified epoxy resin should be from about 5.0 to 30 weight percent to provide a resin having the properties desired to produce the results of the present invention.
Rubber modified epoxy resins prepared through addition polymerization of an epoxy resin and a butadiene rubber or a nitrile rubber exhibit a permanent deformation under a low pressure force, are soft and heat-resistive, yet are highly elastic, possess low dynamic exothermic properties and excellent low-temperature characteristics. As a result, the inventive resin bound magnets exhibit excellent radial compression strength and mechanical properties. In addition, neither rigorous control of the organic solvent nor a vacuum drying process are required. Consequently, the inventive compound of the magnetic material and the rubber modified epoxy resin is highly workable.
FIG. 1 is a schematic flow chart of the method of the invention.
FIG. 2 is a structural formula of the rubbery portion of a modified epoxy resin suitable for use as a binder in the present invention.
The powdered magnetic material of the invention may contain a powdered compound of a rare earth metal, iron and boron, such as, Nd-Fe-B as its principle ingredient. Alternatively, a powdered compound of a rare earth metal and cobalt, such as, Sm-Co, may be used. Still alternatively, the rare earth component of the compound may be a mixture of rare earth elements selected from the group consisting of light rare earth elements and heavy rare earth elements, e.g., La through Lu (atomic numbers 57 through 71), Sc and yttrium (Y). Preferably, the powdered compound contains at least one light rare earth element, such as, neodymium (Nd) or praseodymium (Pr) that is readily available at a relatively low cost. The content of rare earth elements in the compound is preferably between about 12 and 20 atom percent.
The iron (Fe) content of the powdered magnetic material is preferably between about 65 and 82 atom percent, whereas the boron (B) content is advantageously between about 4 and 24 atom percent.
The powdered magnetic material is typically a rare earth element-iron-boron compound which is expressed by the formula:
Nd.sub.x (Fe.sub.1-y B.sub.y).sub.1-c '
where X=0.14 to 0.40 and Y=0.05 to 0.2.
Preferably, the powdered magnetic material has a particle size distribution such that about 0.1 wt. percent or less has a size equal to or greater than about 420 μm, and no more than about 15 wt. % have a particle size equal to or less than about 44 μm. This facilitates mixing the compound with a binder resin material at a high concentration.
The particles of the powdered magnetic material are preferably coated with a rust-preventive agent before mixing and kneading with the binder resin material, since the powdered magnetic material containing rare earth elements, iron and boron, is easily oxidized and has poor corrosion-resistance. Such a surface treatment can significantly improve the corrosion-resistance of the powder and make the process of rust-prevention after molding less troublesome.
While the rust-prevention treatment is optional, the coating process using a triazine derivative, e.g., dibutylamino-triazine-dithiol, as disclosed in Japanese Patent Publication Tokkai Hei No. 1-114006 by the applicant of the present invention, may be advantageously used.
When the powdered magnetic material is subjected to such a surface treatment process, each of the atoms of the heavy metals, i.e., Fe, Nd, of the magnetic material are adsorption-bonded with the dithiol group of the triazine derivative so that the particle is coated with an organic material which is highly rust-preventive. Moreover, the effect of the bridge formation carried by the organic compound and the binder resin, can contribute to improvement in the mechanical strength of the molded body.
A binder resin which can be used in the present invention is the rubber modified epoxy resin wherein the rubbery portion has the structural formula as shown in FIG. 2 wherein m is from 1 to 3, n is 1 to 3, and x is from 1 to 8, prepared by addition polymerization of an epoxy resin and a butadiene rubber or a nitrile rubber.
Another binder resin suitable for use in the present invention has the structural formula: ##STR1## wherein p is 1 to 3, x is 1 to 8, m is 1 to 3 and n is 1 to 3,
A preferred process for carrying out the method of manufacturing the inventive magnet from a powdered magnetic material (or a powdered magnetic material that has been subjected to a corrosion resistent treatment) and a rubber modified epoxy resin as binder, will be described by referring to FIG. 1.
Kneading as used herein includes conditioning, mixing and physically kneading the powdered magnetic material and a binder resin to prepare the material to be molded for a permanent magnet.
In this step, the magnetic powder is coated with a rubber modified epoxy resin prepared by the addition polymerization of an epi-bis type epoxy resin and a butadiene rubber or a nitrile rubber having a rubber content between about 5 and 30 wt. %, and preferably, about 20 wt. %. We have found that when the rubber content of the polymer is less than about 5 wt. % or more than about 30 wt. %, the desirable properties of the resin deteriorate to a level such that the purposes of the invention are not achieved. The amount of binder resin is from 2 to 4 wt. % based on the weight of the magnetic material.
The modified epoxy resin is mixed with a hardening agent and the mixture is dissolved in an organic solvent, e.g., acetone or methyl ethyl ketone, in which it is soluble. The magnetic powder is admixed and kneaded with the solution and the solvent is removed, thereby coating the particles with the binder resin.
More specifically, for preparation of the powdered compound, the binder resin is dissolved in acetone in a non-magnetic mortar and the powdered magnetic material is added to the solution. The mixture is kneaded with a spatula while dry nitrogen gas (N2) is blown into the solvent to prevent oxidation of the powdered magnetic material and to accelerate evaporation of the solvent. Alternatively, a screw, or a floating or soft-mixing apparatus may be used for kneading.
The product obtained from the kneading step is then pulverized in a non-magnetic mortar and passed through a 60-mesh sieve to obtain a powdered compound with even sized particles. Then, a lubricant may be admixed with the sieved powdered compound. Suitable lubricants mixture include calcium stearate, zinc stearate, molybdenum and the like. The amount of lubricant is generally from about 0.01 to 0.5 wt. %. The mixture is then introduced into a metal mold to form a compression molded compound as described below.
The mixture of the sieved compound and calcium stearate is introduced into a compression mold and subjected to a pressure of about 9 ton/cm2 to obtain a ring-shaped or tablet-shaped compression-molded and resin-bound body.
Any unbound magnetic powder left on the surface of the compression molded and resin bound body is removed by means of vacumming.
The molded body is subjected to a heat treatment at 200° C. for approximately 20 minutes for heat setting and to obtain a resin bound magnet.
The prepared resin bound magnet may then subjected to a rust-prevention process using known spraying and electrodeposition, or immersion techniques to produce a finished product. The rust-prevention process may be omitted if the powdered magnetic material has been subjected to a coating process using a triazine derivative as described earlier. However, it is advisable that the resin bound magnet be further subjected to a triazine treatment for the protection of particles whose coating might have been destroyed during the molding process.
This second triazine treatment process uses a triazine derivative similar to or the same as that described above to coat the molded magnet. The operation of coating the molded magnet with an organic material may be conducted by means of immersion, electrodeposition, or spray techniques.
Because the inventive resin bound magnet prepared by the above process contains a highly rigid hard segment in which the molecules are firmly bound together and a soft segment constituted by a highly elastic rubber content, it exhibits a permanent deformation under a low compressive force and is soft and heat-resistive. Yet, the inventive magnet is highly elastic, and possesses a low dynamic exothermic property and excellent low-temperature characteristics. Moreover, the inventive resin bound magnet exhibits excellent radial compression strength and other mechanical properties.
When acetone is used as solvent for the rubber modified epoxy resin at the time of kneading, the kneaded compound can be easily reduced to powder because the rubber modified epoxy resin is essentially unaffected by the acetone in the compound. The compound does not need to be vacuum dried to remove the acetone.
The Table below shows some of the binding characteristics of an epi-bis type epoxy resin containing a rubber modified epoxy resin in varying amounts as well as those of a conventional currently available epoxy resin.
TABLE __________________________________________________________________________ Amount of rubber in polymer conventional in rubber modified epoxy resin (wt. %) unmodified 0 10 20 30 40 60 80 epoxy resin __________________________________________________________________________ radial compression 4.5 5.0 6.3 6.5 7.1 7.1 6.7 4.0 strength (kg/mm.sup.2) specific gravity 5.6 5.5 5.43 5.53 5.62 5.77 5.74 5.6 (g/cm.sup.3) amount filled into 3.3 3.3 3.3 3.0 2.5 1.8 2.3 2.6 mold (g) fluidity (sec) 1.3 1.3 1.3 2.1 ∞ ∞ ∞ 1.5 (BH)max (MGOe) 8.4 8.5 8.5 8.4 8.4 8.4 8.4 overall good excellent excellent good no no no good good good good __________________________________________________________________________ Those materials with a fluidity of ∞ cannot be put into a mold for compression molding
As is apparent from the Table, when a rubber modified epoxy resin is used as the binder resin, the radial compression strength of the final product is remarkably improved without adversely affecting the magnetic characteristics (particularly (BH)max). The binder shows a maximum effect when its rubber modified epoxy resin content is 20 wt. %.
Therefore, when a resin bound magnet prepared by the method of the invention is used for a rotor magnet of an electric motor, it can be easily press fit into the motor. Motors provided with such a resin bound magnet are very light, exhibit excellent magnetic characteristics, and yet, can be produced at reduced manufacturing cost.
Additionally, since the rubber modified epoxy resin is minimally or not affected by the residual organic solvent, such as, acetone, it does not need to be subjected to rigorous control of the residual organic solvent nor a vacuum drying process, and exhibits improved workability after compression molding.
Claims (10)
1. A resin bound magnet comprising a homogenous mixture of a powdered magnetic material and from 2 to 4 weight percent based on the weight of the magnetic material of a cured, rubber-modified epoxy resin wherein the rubber component is about 5 to 30 weight percent of a butadiene or nitrile rubber, based on the weight of the resin.
2. The resin bound magnet of claim 1 wherein the amount of rubber in the resin is about 20% by weight.
3. The resin bound magnet of claim 1 wherein the epoxy resin is an epi-bis type of epoxy resin obtained by the condensation of epichlorhydrin and bis-phenol A.
4. The resin bound magnet of claim 1 wherein the powdered magnetic material comprises a rare earth element iron and boron compound.
5. The resin bound magnet of claim 1 wherein the powdered magnetic material comprises a compound having the formula:
Nd.sub.x (FE.sub.1-y B.sub.y).sub.1-x '
where X=0.14 to 0.40 and Y=0.05 to 0.2.
6. The resin bound magnet of claim 1 wherein the powdered magnetic material comprises a rare earth element and cobalt.
7. The resin bound magnet of claim 1 wherein the powdered magnetic material comprises from about 65 to 82 atom percent iron, from about 4 to 24 atom percent boron, and from about 12 to 20 atom percent of a rare earth element.
8. The resin bound magnet of claim 1 wherein the powdered magnetic material has been treated with a triazine compound to make it corrosion resistant.
9. The resin bound magnet of claim 1 in the form of a rotor magnet.
10. In an electric motor having a rotor magnet therein, the improvement which comprises said magnet being the rotor magnet of claim 9.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1-342994 | 1989-12-28 | ||
JP1342994A JPH03201508A (en) | 1989-12-28 | 1989-12-28 | Manufacture of resin-bonded magnet |
Publications (1)
Publication Number | Publication Date |
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US5176842A true US5176842A (en) | 1993-01-05 |
Family
ID=18358119
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US07/635,270 Expired - Lifetime US5176842A (en) | 1989-12-28 | 1990-12-28 | Method of manufacturing a resin bound magnet |
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US (1) | US5176842A (en) |
JP (1) | JPH03201508A (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5393445A (en) * | 1991-12-26 | 1995-02-28 | Daido Tokushuko Kabushiki Kaisha | Rare-earth bonded magnet, material and method for manufacturing the same |
EP0693633A3 (en) * | 1994-07-22 | 1996-05-08 | Ti Matrix Eng Ltd | Electromagnetically controlled permanent magnet brake |
US6001272A (en) * | 1996-03-18 | 1999-12-14 | Seiko Epson Corporation | Method for producing rare earth bond magnet, composition for rare earth bond magnet, and rare earth bond magnet |
US20030189475A1 (en) * | 2002-04-09 | 2003-10-09 | The Electrodyne Company, Inc. | Bonded permanent magnets |
US6790378B2 (en) | 2001-10-05 | 2004-09-14 | R. William Graham | Coating composition having magnetic properties |
CN100369700C (en) * | 2005-12-22 | 2008-02-20 | 株洲钻石切削刀具股份有限公司 | Plasticizer for carbide alloy production |
US20140170014A1 (en) * | 2012-12-13 | 2014-06-19 | Korea Institute Of Machinery & Materials | Method for producing magnetic powder and magnet |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4181003B2 (en) * | 2003-09-29 | 2008-11-12 | 三菱電機株式会社 | Permanent magnet forming device |
Citations (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3371044A (en) * | 1963-01-25 | 1968-02-27 | Westinghouse Electric Corp | Ferrite magnets |
US3585141A (en) * | 1969-05-05 | 1971-06-15 | Du Pont | Stabilization of chromium dioxide by monomeric cyclic amines |
JPS505899A (en) * | 1973-05-18 | 1975-01-22 | ||
US4689163A (en) * | 1986-02-24 | 1987-08-25 | Matsushita Electric Industrial Co., Ltd. | Resin-bonded magnet comprising a specific type of ferromagnetic powder dispersed in a specific type of resin binder |
JPS63284808A (en) * | 1987-05-18 | 1988-11-22 | Nippon Telegr & Teleph Corp <Ntt> | Compound semiconductor layer |
JPH01114006A (en) * | 1987-10-28 | 1989-05-02 | Sankyo Seiki Mfg Co Ltd | Manufacture of resin bond type magnet |
US4878978A (en) * | 1986-06-19 | 1989-11-07 | Ashland Oil, Inc. | Bonding method employing high performance induction curable two-component structural adhesive with nonsagging behavior |
US4981635A (en) * | 1988-02-29 | 1991-01-01 | Matsushita Electric Industrial Co., Ltd. | Methods for producing a resin-bonded magnet |
US5096741A (en) * | 1988-06-27 | 1992-03-17 | Kabushiki Kaisha Sankyo Seiki Seisakusho | Corrosionproof coating material and method for formation of coating therewith |
US5128215A (en) * | 1989-05-19 | 1992-07-07 | Minnesota Mining & Manufacturing Company | Magnetic recording media binder resin comprising a mixture of a straight block copolymer and a star block copolymer |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5721450A (en) * | 1980-07-11 | 1982-02-04 | Toho Rayon Co Ltd | Epoxy resin composition |
JPS62264602A (en) * | 1986-05-13 | 1987-11-17 | Seiko Epson Corp | Ferromagnetic resin composite |
-
1989
- 1989-12-28 JP JP1342994A patent/JPH03201508A/en active Pending
-
1990
- 1990-12-28 US US07/635,270 patent/US5176842A/en not_active Expired - Lifetime
Patent Citations (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3371044A (en) * | 1963-01-25 | 1968-02-27 | Westinghouse Electric Corp | Ferrite magnets |
US3585141A (en) * | 1969-05-05 | 1971-06-15 | Du Pont | Stabilization of chromium dioxide by monomeric cyclic amines |
JPS505899A (en) * | 1973-05-18 | 1975-01-22 | ||
US4689163A (en) * | 1986-02-24 | 1987-08-25 | Matsushita Electric Industrial Co., Ltd. | Resin-bonded magnet comprising a specific type of ferromagnetic powder dispersed in a specific type of resin binder |
US4878978A (en) * | 1986-06-19 | 1989-11-07 | Ashland Oil, Inc. | Bonding method employing high performance induction curable two-component structural adhesive with nonsagging behavior |
JPS63284808A (en) * | 1987-05-18 | 1988-11-22 | Nippon Telegr & Teleph Corp <Ntt> | Compound semiconductor layer |
JPH01114006A (en) * | 1987-10-28 | 1989-05-02 | Sankyo Seiki Mfg Co Ltd | Manufacture of resin bond type magnet |
US4981635A (en) * | 1988-02-29 | 1991-01-01 | Matsushita Electric Industrial Co., Ltd. | Methods for producing a resin-bonded magnet |
US5096741A (en) * | 1988-06-27 | 1992-03-17 | Kabushiki Kaisha Sankyo Seiki Seisakusho | Corrosionproof coating material and method for formation of coating therewith |
US5128215A (en) * | 1989-05-19 | 1992-07-07 | Minnesota Mining & Manufacturing Company | Magnetic recording media binder resin comprising a mixture of a straight block copolymer and a star block copolymer |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5393445A (en) * | 1991-12-26 | 1995-02-28 | Daido Tokushuko Kabushiki Kaisha | Rare-earth bonded magnet, material and method for manufacturing the same |
EP0693633A3 (en) * | 1994-07-22 | 1996-05-08 | Ti Matrix Eng Ltd | Electromagnetically controlled permanent magnet brake |
US6001272A (en) * | 1996-03-18 | 1999-12-14 | Seiko Epson Corporation | Method for producing rare earth bond magnet, composition for rare earth bond magnet, and rare earth bond magnet |
US6790378B2 (en) | 2001-10-05 | 2004-09-14 | R. William Graham | Coating composition having magnetic properties |
US20030189475A1 (en) * | 2002-04-09 | 2003-10-09 | The Electrodyne Company, Inc. | Bonded permanent magnets |
US6707361B2 (en) | 2002-04-09 | 2004-03-16 | The Electrodyne Company, Inc. | Bonded permanent magnets |
CN100369700C (en) * | 2005-12-22 | 2008-02-20 | 株洲钻石切削刀具股份有限公司 | Plasticizer for carbide alloy production |
US20140170014A1 (en) * | 2012-12-13 | 2014-06-19 | Korea Institute Of Machinery & Materials | Method for producing magnetic powder and magnet |
Also Published As
Publication number | Publication date |
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JPH03201508A (en) | 1991-09-03 |
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